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临床试验/NL-OMON54927
NL-OMON54927招募中2 期

Pathophysiological relevance of IRON deficiency and related mitochondrial dysfunction in Heart Failure with Preserved Ejection Fraction (IRON-HFpEF) - IRON-HFpEF

Vrije Universiteit Medisch Centrum0 个研究点目标入组 45 人开始时间: 待定最近更新:
适应症

试验速览

阶段
2 期
状态
招募中
入组人数
45

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 至 99(—)

入选标准

  • 1. Diagnosis of heart failure with preserved ejection fraction
  • a. signs/and symptoms of heartfailure (NYHA II or higher)
  • b. Left ventricular ejection fraction >=50%
  • c. evidence of left ventricular diastolic dysfunction:
  • -pulmonary capillary wedge pressure (PCWP) at rest >= 15mmHg and/or PCWP
  • leg-raise >= 20mmHg and/or PCWP during exercise >= 25mmHg
  • or if no right heart catheterisation has been performed:
  • -HFpEf score >= 6;
  • -diastolic dysfunction grade II or higher on echocardiogram + NTproBNP of
  • >125 pg/mL
  • d. no other significant cardiac (e.g. significant valvular disease) or
  • extra-cardiac con-dition (e.g. severe COPD) that explains symptoms
  • 2. Optimal medical treatment
  • 3. Clinically stable
  • 4. Iron deficient (ferritin <100pg/L or ferritin 100-300pg/L and transferrin
  • saturation or TSAT <20%).
  • 5. Hemoglobin >9.0 g/dL (5.6 mmol/L)

排除标准

  • 1. No informed consent
  • 2. Contra indication ferric carboxy maltose
  • a. known allergic reaction to product; b. clinical signs of an acute infection;
  • c. conditions with high risk for an allergic reaction: severe asthma or eczema,
  • systemic lu-pus erhytematosus, rheumatoid arthritis or concurrent use of
  • significant immunosuppres-sive therapy (With an exception of patients who
  • previously have received intravenous iron without allergic response. As
  • allergic reaction is unlikely in these patients).; severe liver disease
  • 3. History of (previous 2 months) or planned use of intravenous/oral iron,
  • erythro-poietin or blood transfusion
  • 4. Indication for iron supplementation according to Dutch guidelines.
  • 5. Acute coronary syndrome, TIA/CVA, PCI/CABG/valve replacement or any major
  • surgery within 3 months prior;
  • 6. Unable to undergo the complete study protocol (i.e. right heart
  • catheterisation, 6 minute walk distance)
  • 7. Indication for iron supplementation

研究者

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